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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 708504Generated: November 1, 2026

Benzyl((2R,3S)-2-((4-(((tert-butyldimethylsilyl)oxy)methyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamate → Benzyl((2R,3S)-2-((4-(hydroxymethyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamate

https://huagongshe.com/reaction/708504

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl((2R,3S)-2-((4-(((tert-butyldimethylsilyl)oxy)methyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamateHCID 131733718—
SolventMethanolHCID 887—
ProductBenzyl((2R,3S)-2-((4-(hydroxymethyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamateHCID 118411384—

Reaction Steps

To a solution of benzyl ((2R,3S)-2-((4-(((tert-butyldimethylsilyl)oxy)methyl)-2H-1,2,3-triazol-2-yl)methyl)-4-oxoazetidin-3-yl)carbamate (500 mg, 1.12 mmol) in MeOH (15 mL) was added DOWEX-50W-X4 100-200 (1 g, 1.12 mmol) resin. After stirring at rt for 3 h, the reaction mixture was filtered, and the filtrate was concentrated in vacuo to give the title compound (assume quantitative). LCMS: Rt=0.51 min, m/z=332.1 (M+1) Method 2m_acidic.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174978B2
Source datasetuspto-grants-2015_11
ORD IDord-9ed3b585e9ee4d87b7edec5ccd52295d
Source noteuspto-grants-2015_11